Clinical Trials Directory

Trials / Completed

CompletedNCT04487028

Dysphagia in Thoracic Surgical Patients

Dysphagia in Thoracic Surgical Patients: Incidence, Risk-factors, and Health Related Outcomes

Status
Completed
Phase
Study type
Observational
Enrollment
61 (actual)
Sponsor
University of Florida · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

The proposed study seeks to determine the incidence of dysphagia and vocal fold mobility impairment (VFMI) in individuals undergoing throacic surgical procedures. It also seeks to determine the impact of postoperative swallowing impairment on health-related outcomes.

Detailed description

Swallowing impairment and VFMI are common, yet often overlooked, complications of thoracic surgical procedures. The true incidence of both dysphagia and VFMI in this patient population is unclear due to a lack of rigorous study using instrumental assessment techniques and validated outcomes in all patents undergoing thoracic surgery. The study is therefore aimed to determine the incidence of dysphagia and VFMI in this patient population and to characterize impairment profiles related to swallowing safety and efficiency. In addition, the study is also aimed to assess the relative impact of VFMI and dysphagia on health-related outcomes such as length of hospital stay, pneumonia, sepsis, reintubation, and discharge status

Conditions

Interventions

TypeNameDescription
PROCEDUREFiberoptic Endoscopic Evaluation of SwallowingThis procedure involves inserting a flexible laryngoscope that contains a light source and video camera on the end through the open passage of the nose towards the back of the throat in order to visualize the swallowing mechanism.

Timeline

Start date
2020-08-25
Primary completion
2021-08-13
Completion
2021-11-22
First posted
2020-07-27
Last updated
2021-11-24

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT04487028. Inclusion in this directory is not an endorsement.